Showing posts with label Christopher Russell. Show all posts
Showing posts with label Christopher Russell. Show all posts

Friday, July 7, 2017

Abstract-On-chip Terahertz-Frequency Measurements of Liquids



Anal. Chem., Just Accepted Manuscript
DOI: 10.1021/acs.analchem.7b01235
Publication Date (Web): July 6, 2017
Copyright © 2017 American Chemical Society


Terahertz-frequency-range measurements can offer potential insight into the picosecond dynamics, and therefore function, of many chemical systems. There is a need to develop technologies capable of performing such measurements in aqueous and polar environments, particularly when it is necessary to maintain the full functionality of biological samples. In this study, we present a proof-of-concept technology comprising an on-chip planar Goubau line, integrated with a microfluidic channel, which is capable of low-loss, terahertz-frequency-range spectroscopic measurements of liquids. We also introduce a mathematical model that accounts for changes in the electric field distribution around the waveguide, allowing accurate, frequency-dependent liquid parameters to be extracted. We demonstrate the sensitivity of this technique by measuring a homologous alcohol series across the 0.1-0.8 THz frequency range.

Sunday, November 13, 2016

Abstract-Free-space terahertz radiation from a LT-GaAs-on-quartz large-area photoconductive emitter


Wednesday, July 24, 2013

Abstract-The effect of molecular size and particle shape on the terahertz absorption of a homologous series of tetraalkylammonium salts.



The absorption coefficient and refractive index have been measured for a homologous series of tetraalkylammonium bromides over the frequency range 0.3 to 5.5 THz. Spectral features are found to shift to lower frequencies as the molecular mass is increased, as expected. However, in order to understand the detailed structure of the observed spectral features, density functional perturbation theory calculations have been performed on the first four crystalline compounds in the series. From these calculations we find that each spectrum is dominated by three translatory modes involving asymmetric motion of the ammonium cation and bromine counter-ion, although the overall number of active modes increases with increasing molecular size. The experimentally observed absorption is not completely described by the infrared active phonon modes alone. We show that it is also necessary to include the coupling of the phonon modes with the macroscopic field generated by the collective displacement of the vibrating ions and we have applied an effective medium theory which accounts for particle shape to allow for this effect in the calculation of the terahertz spectra.